The Centre for Applied Genomics (TCAG) at The Hospital for Sick Children is now offering whole genome sequencing on the Illumina HiSeq X platform. TCAG is the first lab in Canada to offer this service at the most competitive pricing. The whole genome sequencing service is available for human, as well as any other species. The standard service includes sample quality control, library preparation, sequencing to a minimum depth of 30x mean coverage, and the provision of FASTQ (all species), BAM and VCF (for human and mouse) files, including SNVs and indel variants.
For more information, please contact Dr. Sergio Pereira (firstname.lastname@example.org).